Genomics

Dataset Information

0

Diploid genome architecture revealed by multi-omic data of hybrid mice


ABSTRACT: While mammalian genomes are diploid, previous studies extensively investigated the average chromatin architectures without considering the differences between homologous chromosomes. Here we generated Hi-C, ChIP-seq and RNA-seq datasets from CD4 T cells of B6, Cast and hybrid mice, to investigate the diploid chromatin organization and epigenetic regulation. Our data indicate that inter-chromosomal interaction patterns between homologous chromosomes are similar and the similarity is highly correlated with their allelic co-expression levels. Reconstruction of 3D nucleus revealed that distances of the homologous chromosomes to the center of nucleus are almost the same. The inter-chromosomal interactions at centromere-ends are significantly weaker than those at telomere-ends, suggesting that they are located in different regions within the chromosome territories. The majority of A|B compartments or topologically associated domains (TADs) are consistent between B6 and Cast. We found 58% of the haploids in hybrids maintain their parental compartment status at B6/Cast divergent compartments due to cis-effect. About 95% of the trans-effected B6/Cast divergent compartments converge to the same compartment status potentially due to a shared cellular environment. We showed the differentially expressed genes between the two haploids in hybrid were associated with either genetic or epigenetic effects. In summary, our multi-omics data from the hybrid mice provided haploid-specific information on the 3D nuclear architecture and a rich resource for further understanding the epigenetic regulation of haploid-specific gene expression.

ORGANISM(S): Mus musculus

PROVIDER: GSE132898 | GEO | 2020/07/05

REPOSITORIES: GEO

Similar Datasets

2009-08-12 | GSE17578 | GEO
2010-05-15 | E-GEOD-17578 | biostudies-arrayexpress
2017-10-04 | GSE95069 | GEO
2012-11-21 | E-GEOD-39406 | biostudies-arrayexpress
2014-04-10 | E-GEOD-56465 | biostudies-arrayexpress
2018-09-28 | GSE119727 | GEO
2014-04-10 | GSE56465 | GEO
2015-02-04 | E-GEOD-61553 | biostudies-arrayexpress
2015-12-09 | E-GEOD-60934 | biostudies-arrayexpress
2010-01-30 | GSE20108 | GEO